Canonical Allele Identifier: CA353249981

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835163A>T (hg19) ; chr3:g.53801136A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801136A>T , CM000665.2:g.53801136A>T	GRCh38
NC_000003.11:g.53835163A>T , CM000665.1:g.53835163A>T	GRCh37
NC_000003.10:g.53810203A>T	NCBI36
NG_032999.1:g.311088A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5179A>T	ENSP00000418014.2:p.Thr1727Ser
ENST00000636633.2:n.2194-76A>T
ENST00000636999.2:n.554A>T
ENST00000288139.11:c.5179A>T MANE Plus Clinical	ENSP00000288139.3:p.Thr1727Ser
ENST00000350061.11:c.5119A>T MANE Select	ENSP00000288133.5:p.Thr1707Ser
ENST00000422281.7:c.5074A>T	ENSP00000409174.2:p.Thr1692Ser
ENST00000636448.1:c.1316-76A>T
ENST00000636570.1:c.5074A>T	ENSP00000490183.1:p.Thr1692Ser
ENST00000636629.1:n.475A>T
ENST00000636633.1:n.2194-76A>T
ENST00000636999.1:n.546A>T
ENST00000637424.1:c.5146A>T	ENSP00000489769.1:p.Thr1716Ser
ENST00000288139.8:c.5179A>T	ENSP00000288139.3:p.Thr1727Ser
ENST00000350061.9:c.5119A>T	ENSP00000288133.5:p.Thr1707Ser
ENST00000422281.6:c.5074A>T	ENSP00000409174.2:p.Thr1692Ser
ENST00000481478.1:c.4198A>T	ENSP00000418014.1:p.Thr1400Ser
NM_000720.3:c.5179A>T	NP_000711.1:p.Thr1727Ser
NM_001128839.2:c.5074A>T	NP_001122311.1:p.Thr1692Ser
NM_001128840.2:c.5119A>T	NP_001122312.1:p.Thr1707Ser
XM_005265448.2:c.5074A>T	XP_005265505.1:p.Thr1692Ser
XM_011534094.1:c.5374A>T	XP_011532396.1:p.Thr1792Ser
XM_011534095.1:c.5263A>T	XP_011532397.1:p.Thr1755Ser
XM_011534096.1:c.5185A>T	XP_011532398.1:p.Thr1729Ser
XM_011534097.1:c.4837A>T	XP_011532399.1:p.Thr1613Ser
XM_011534098.1:c.4837A>T	XP_011532400.1:p.Thr1613Ser
XM_011534099.1:c.4462A>T	XP_011532401.1:p.Thr1488Ser
XM_011534100.1:c.5269A>T	XP_011532402.1:p.Thr1757Ser
XM_005265448.3:c.5074A>T	XP_005265505.1:p.Thr1692Ser
XM_011534094.2:c.5374A>T	XP_011532396.1:p.Thr1792Ser
XM_011534096.2:c.5185A>T	XP_011532398.1:p.Thr1729Ser
XM_011534097.2:c.4837A>T	XP_011532399.1:p.Thr1613Ser
XM_011534099.2:c.4462A>T	XP_011532401.1:p.Thr1488Ser
XM_011534100.2:c.5269A>T	XP_011532402.1:p.Thr1757Ser
XM_017007137.1:c.5374A>T	XP_016862626.1:p.Thr1792Ser
XM_017007138.1:c.5371A>T	XP_016862627.1:p.Thr1791Ser
XM_017007139.1:c.5374A>T	XP_016862628.1:p.Thr1792Ser
XM_017007140.1:c.5314A>T	XP_016862629.1:p.Thr1772Ser
XM_017007141.1:c.5314A>T	XP_016862630.1:p.Thr1772Ser
XM_017007142.1:c.5290A>T	XP_016862631.1:p.Thr1764Ser
XM_017007143.1:c.5290A>T	XP_016862632.1:p.Thr1764Ser
XM_017007144.1:c.5290A>T	XP_016862633.1:p.Thr1764Ser
XM_017007145.1:c.5245A>T	XP_016862634.1:p.Thr1749Ser
NM_001128840.3:c.5119A>T MANE Select	NP_001122312.1:p.Thr1707Ser
NM_000720.4:c.5179A>T MANE Plus Clinical	NP_000711.1:p.Thr1727Ser
NM_001128839.3:c.5074A>T	NP_001122311.1:p.Thr1692Ser